C. Muñoz

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Prognostic impact of chromosomal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemia patients. A study by the spanish group of myelodysplastic syndromes

J. Esteve, E. Campo, F. Solé, 2016, Genes, chromosomes & cancer.

Do we need to do fluorescence in situ hybridization analysis in myelodysplastic syndromes as often as we do?

E. Campo, D. Costa, M. Rozman, 2010, Leukemia research.

Response to lenalidomide in patients with myelodysplastic syndrome with deletion 5q: clinical and cytogenetic analysis of a single centre series

E. Campo, D. Costa, R. Coutinho, 2010, Annals of Hematology.

TERT and AURKA gene copy number gains enhance the detection of acral lentiginous melanomas by fluorescence in situ hybridization.

J. Malvehy, S. Puig, A. Valera, 2014, The Journal of molecular diagnostics : JMD.

Refining the Diagnosis and Prognostic Categorization of Acute Myeloid Leukemia Patients with an Integrated Use of Cytogenetic and Molecular Studies

J. Esteve, E. Campo, D. Colomer, 2012, Acta Haematologica.

Clonal evolution in chronic lymphocytic leukemia: Analysis of correlations with IGHV mutational status, NOTCH1 mutations and clinical significance

A. López-Guillermo, E. Campo, N. Villamor, 2013, Genes, chromosomes & cancer.

TERT gene amplification is associated with poor outcome in acral lentiginous melanoma.

J. Malvehy, S. Puig, A. García-Herrera, 2014, Journal of the American Academy of Dermatology.

Refining the Breakpoints of Three New Translocations Identified in Myelodysplastic Syndromes

E. Campo, F. Solé, D. Costa, 2015, Acta Haematologica.

A new genetic abnormality leading to TP53 gene deletion in chronic lymphocytic leukaemia

E. Campo, E. Montserrat, N. Villamor, 2012, British journal of haematology.

Different distribution of NOTCH1 mutations in chronic lymphocytic leukemia with isolated trisomy 12 or associated with other chromosomal alterations

A. López-Guillermo, E. Campo, E. Montserrat, 2012, Genes, chromosomes & cancer.

High levels of global DNA methylation are an independent adverse prognostic factor in a series of 90 patients with de novo myelodysplastic syndrome.

J. Esteve, D. Costa, A. Navarro, 2014, Leukemia research.

TERT and AURKA gene copy number gains enhance the detection of acral lentiginous melanomas by fluorescence in situ hybridization.

J. Malvehy, S. Puig, A. García-Herrera, 2014, The Journal of molecular diagnostics : JMD.

Prognostic impact of chromosomal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemia patients. A study by the spanish group of myelodysplastic syndromes

J. Esteve, E. Campo, F. Solé, 2016, Genes, chromosomes & cancer.

Reciprocal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemias: Review of 5,654 patients with an evaluable karyotype

E. Campo, F. Solé, D. Costa, 2013, Genes, chromosomes & cancer.

Refining the Breakpoints of Three New Translocations Identified in Myelodysplastic Syndromes

E. Campo, F. Solé, D. Costa, 2015, Acta Haematologica.